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Maas & Peither AG
Karlstrasse 2
79650 Schopfheim, Germany

Phone +49 (0)7622 666 86-70
Fax     +49 (0)7622 666 86-77


Maas & Peither America, Inc.
1060 First Avenue, Suite 400
King of Prussia, PA 19406, USA

Phone +1 (610) 768-8028
Fax     +1 (610) 337-9548


TOP 5 GMP Downloads

1. Quality Agreement
Defines framework conditions and processes between contract givers and contract acceptors in order to meet mandatory quality criteria.


2. GDP Audit Checklist
More than 700 questions with reference to regulations for preparing and carrying out GDP audits.


3. GMP Audit Checklist
The GMP Audit Checklist works great for both sides - the auditor and the inspected company.


4. Technical Agreement
and Delimination of Pharmaceutical Responsibilities.


5. A Process Approach to Pharmaceutical Quality Systems
A Guide to ICH Q10 Compliance


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You need GMP information that is reviewed by GMP experts and is guaranteed reliable. Our advisory board includes members from US, Europe and Japan. They supervise the content and development of the GMP MANUAL. More than 50 experts around the world write articles that are peer-reviewed. You get the best GMP information when you need it.

Our panel has the right background and credentials to make sure that we provide the highest level of expertise and knowledge to the industry:



1976-1980 Northern Illinois University, DeKalb, IL (Biology/Chemistry) B.S.

1984-1988 Lake Forest School of Management, Lake Forest, IL, M.B.A.

2003-2009 ASQ: Quality Management Certification

2005-2009 RAPS (Regulatory Affairs Professional Society): Regulatory Affairs Certification

06/2007-01/2009 Medical Products Group (MPG): DVP Quality/RA/QA/Compliance
Support all eight MPG Division for quality and regulatory support. In addition directly support FDA Inspection Readiness Programs. Quality system Initiative for MPG, including QA Council and Executive Management Review.

01/2009-07/2009 Abbott Quality and Regulatory (AQR): DVP Quality System Continuous Improvement
Global AQR responsibility for Inspection Readiness Program, IT QA/RA Roadmap including development and implementation of the IT tools.

07/2009-Present Abbott Quality and Regulatory (AQR): DVP Global Strategic Regulatory
Global Strategic Regulatory provides leadership, direction and support for the planning, development, implementation and maintenance of short and long term corporate-wide effective strategies and programs related to critical global regulatory and quality initiatives, issues identified internally, and externally through industry groups and by the regulatory agencies.

Publications at Maas & Peither GMP Publishing: